Canonical Allele Identifier: PA915964774
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4029
ClinVar RCV Id: RCV000004244 RCV000055768 RCV001785448 RCV004018551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Asp645Glu
CA116610
NM_001079804.3:c.1935C>A
CA401369909
NM_001079804.3:c.1935C>G